Parp16 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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36 records found for search term Parp16

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401750604	CV2689469	single nucleotide variant	NM_001316943.2(PARP16):c.14G>A (p.Gly5Asp)	not specified [RCV004308314]	uncertain significance	15	65286413	65286413	Human		name
598129305	CV3888599	single nucleotide variant	NM_001316943.2(PARP16):c.135G>C (p.Ala45=)	not provided [RCV005244773]	likely benign	15	65286292	65286292	Human		name
401743529	CV2687975	single nucleotide variant	NM_001316943.2(PARP16):c.37G>A (p.Ala13Thr)	not specified [RCV004305053]	uncertain significance	15	65286390	65286390	Human		name
407479694	CV3466619	single nucleotide variant	NM_001316943.2(PARP16):c.89C>T (p.Ala30Val)	not specified [RCV004664198]	uncertain significance	15	65286338	65286338	Human		name
597674964	CV3568147	single nucleotide variant	NM_001316943.2(PARP16):c.35C>G (p.Ala12Gly)	not specified [RCV004830242]	uncertain significance	15	65286392	65286392	Human		name
598244042	CV4002113	single nucleotide variant	NM_001316943.2(PARP16):c.33G>C (p.Glu11Asp)	not specified [RCV005383688]	uncertain significance	15	65286394	65286394	Human		name
15186544	CV726208	single nucleotide variant	NM_001316943.2(PARP16):c.960G>A (p.Ala320=)	not provided [RCV000887005]	benign	15	65259416	65259416	Human		name
156343966	CV2229581	single nucleotide variant	NM_001316943.2(PARP16):c.143C>T (p.Ala48Val)	not specified [RCV004103400]	uncertain significance	15	65286284	65286284	Human		name
156121291	CV2240804	single nucleotide variant	NM_001316943.2(PARP16):c.145C>T (p.Arg49Cys)	not specified [RCV004102101]	uncertain significance	15	65286282	65286282	Human		name
156266943	CV2372571	single nucleotide variant	NM_001316943.2(PARP16):c.130C>T (p.Pro44Ser)	not specified [RCV004219363]	uncertain significance	15	65286297	65286297	Human		name
401717834	CV2704036	single nucleotide variant	NM_001316943.2(PARP16):c.290T>C (p.Ile97Thr)	not specified [RCV004308921]	uncertain significance	15	65270957	65270957	Human		name
401893311	CV2756540	single nucleotide variant	NM_001316943.2(PARP16):c.208G>C (p.Glu70Gln)	not specified [RCV004345068]	uncertain significance	15	65271039	65271039	Human		name
407479699	CV3466621	single nucleotide variant	NM_001316943.2(PARP16):c.179C>A (p.Ala60Glu)	not specified [RCV004664199]	uncertain significance	15	65271068	65271068	Human		name
598244050	CV4002115	single nucleotide variant	NM_001316943.2(PARP16):c.188G>A (p.Ser63Asn)	not specified [RCV005383689]	uncertain significance	15	65271059	65271059	Human		name
156398940	CV2194879	single nucleotide variant	NM_001316943.2(PARP16):c.616G>A (p.Gly206Ser)	not specified [RCV004075411]	uncertain significance	15	65263224	65263224	Human		name
156052249	CV2238186	single nucleotide variant	NM_001316943.2(PARP16):c.494A>G (p.Asn165Ser)	not specified [RCV004111183]	uncertain significance	15	65266587	65266587	Human		name
156281930	CV2252367	single nucleotide variant	NM_001316943.2(PARP16):c.504C>G (p.His168Gln)	not specified [RCV004116213]	uncertain significance	15	65266577	65266577	Human		name
156038423	CV2313640	single nucleotide variant	NM_001316943.2(PARP16):c.524C>T (p.Ser175Phe)	not specified [RCV004157572]	uncertain significance	15	65263316	65263316	Human		name
156280903	CV2316016	single nucleotide variant	NM_001316943.2(PARP16):c.592C>T (p.His198Tyr)	not specified [RCV004172072]	uncertain significance	15	65263248	65263248	Human		name
155972948	CV2320896	single nucleotide variant	NM_001316943.2(PARP16):c.541A>G (p.Thr181Ala)	not specified [RCV004172710]	uncertain significance	15	65263299	65263299	Human		name
156199896	CV2331474	single nucleotide variant	NM_001316943.2(PARP16):c.571C>G (p.Leu191Val)	not specified [RCV004184106]	uncertain significance	15	65263269	65263269	Human		name
156304791	CV2338556	single nucleotide variant	NM_001316943.2(PARP16):c.670A>C (p.Lys224Gln)	not provided [RCV004695581]\|not specified [RCV004189011]	uncertain significance	15	65263170	65263170	Human		name
156254472	CV2359224	single nucleotide variant	NM_001316943.2(PARP16):c.413T>C (p.Phe138Ser)	not specified [RCV004212518]	uncertain significance	15	65266668	65266668	Human		name
156262346	CV2376966	single nucleotide variant	NM_001316943.2(PARP16):c.652A>G (p.Ile218Val)	not specified [RCV004229652]	uncertain significance	15	65263188	65263188	Human		name
329392064	CV2445274	single nucleotide variant	NM_001316943.2(PARP16):c.640G>A (p.Val214Met)	not specified [RCV004263902]	uncertain significance	15	65263200	65263200	Human		name
401726717	CV2677319	single nucleotide variant	NM_001316943.2(PARP16):c.662C>T (p.Pro221Leu)	not specified [RCV004295935]	uncertain significance	15	65263178	65263178	Human		name
401753579	CV2722517	single nucleotide variant	NM_001316943.2(PARP16):c.743G>A (p.Gly248Glu)	not specified [RCV004322902]	uncertain significance	15	65260975	65260975	Human		name
405773165	CV3364455	single nucleotide variant	NM_001316943.2(PARP16):c.917G>A (p.Ser306Asn)	not specified [RCV004502640]	uncertain significance	15	65259459	65259459	Human		name
407518349	CV3466620	single nucleotide variant	NM_001316943.2(PARP16):c.646G>A (p.Glu216Lys)	not specified [RCV004650972]	uncertain significance	15	65263194	65263194	Human		name
597719607	CV3568148	single nucleotide variant	NM_001316943.2(PARP16):c.400G>C (p.Ala134Pro)	not specified [RCV004841769]	uncertain significance	15	65266681	65266681	Human		name
597674974	CV3568149	single nucleotide variant	NM_001316943.2(PARP16):c.814T>G (p.Ser272Ala)	not specified [RCV004830243]	uncertain significance	15	65260904	65260904	Human		name
597719617	CV3568150	single nucleotide variant	NM_001316943.2(PARP16):c.811T>A (p.Tyr271Asn)	not specified [RCV004841770]	uncertain significance	15	65260907	65260907	Human		name
597719627	CV3568151	single nucleotide variant	NM_001316943.2(PARP16):c.826C>G (p.Pro276Ala)	not specified [RCV004841771]	uncertain significance	15	65260892	65260892	Human		name
598244036	CV4002110	single nucleotide variant	NM_001316943.2(PARP16):c.716G>A (p.Arg239Gln)	not specified [RCV005383687]	uncertain significance	15	65261002	65261002	Human		name
598185184	CV4002111	single nucleotide variant	NM_001316943.2(PARP16):c.749T>A (p.Ile250Asn)	not specified [RCV005395569]	uncertain significance	15	65260969	65260969	Human		name
598185188	CV4002112	single nucleotide variant	NM_001316943.2(PARP16):c.434G>A (p.Arg145Gln)	not specified [RCV005395570]	uncertain significance	15	65266647	65266647	Human		name

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